Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2908
Gene Symbol: NR3C1
NR3C1
0.400 Biomarker phenotype CTD_human Female pseudohermaphroditism caused by a novel homozygous missense mutation of the GR gene. 11932321 2002
Entrez Id: 2908
Gene Symbol: NR3C1
NR3C1
0.400 Biomarker phenotype HPO
Entrez Id: 154
Gene Symbol: ADRB2
ADRB2
0.310 GeneticVariation phenotype LHGDN The influence of the AA 16 beta 2-adrenoceptor polymorphism on systemic and airway responses in asthma. 17292646 2008
Entrez Id: 154
Gene Symbol: ADRB2
ADRB2
0.310 Biomarker phenotype CTD_human The influence of the AA 16 beta 2-adrenoceptor polymorphism on systemic and airway responses in asthma. 17292646 2008
Entrez Id: 154
Gene Symbol: ADRB2
ADRB2
0.310 Biomarker phenotype CTD_human Debrisoquine phenotype and the pharmacokinetics and beta-2 receptor pharmacodynamics of metoprolol and its enantiomers. 1848636 1991
Entrez Id: 154
Gene Symbol: ADRB2
ADRB2
0.310 Biomarker phenotype CTD_human Beta-2-adrenoceptor-mediated hypokalemia and its abolishment by oxprenolol. 2826064 1987
Entrez Id: 4879
Gene Symbol: NPPB
NPPB
0.300 Biomarker phenotype CTD_human Low-dose nesiritide improves renal function in heart failure patients following acute myocardial infarction. 20339970 2010
Entrez Id: 5443
Gene Symbol: POMC
POMC
0.300 Biomarker phenotype CTD_human Adrenocorticotrophin-induced hypertension: effects of mineralocorticoid and glucocorticoid receptor antagonism. 10100081 1999
Entrez Id: 5443
Gene Symbol: POMC
POMC
0.300 Biomarker phenotype CTD_human Colonic adenocarcinoma associated ectopic ACTH secretion: a case history. 8562174 1995
Entrez Id: 5443
Gene Symbol: POMC
POMC
0.300 Biomarker phenotype CTD_human ACTH revisited: effective treatment for acute crystal induced synovitis in patients with multiple medical problems. 8035395 1994
Entrez Id: 5443
Gene Symbol: POMC
POMC
0.300 Biomarker phenotype CTD_human [Treatment of infantile spasms with long-term low dose ACTH]. 1327015 1992
Entrez Id: 6750
Gene Symbol: SST
SST
0.300 Therapeutic phenotype CTD_human Effects of somatostatin and oral potassium administration on terbutaline-induced hypokalemia. 2563217 1989
Entrez Id: 183
Gene Symbol: AGT
AGT
0.300 Therapeutic phenotype CTD_human Factitious Bartter's syndrome induced by surreptitious intake of furosemide. 7182184 1982
Entrez Id: 5443
Gene Symbol: POMC
POMC
0.300 Biomarker phenotype CTD_human Chronic potentiation of vasoconstrictor hypertension by adrenocorticotropic hormone. 6279499 1982
Entrez Id: 5443
Gene Symbol: POMC
POMC
0.300 Biomarker phenotype CTD_human Syndrome of inappropriate ADH secretion concealed by hypokalaemia due to ectopic ACTH production. 6258369 1981
Entrez Id: 5443
Gene Symbol: POMC
POMC
0.300 Biomarker phenotype CTD_human ACTH therapy in infantile spasms: side effects. 6254450 1980
Entrez Id: 3630
Gene Symbol: INS
INS
0.300 Biomarker phenotype CTD_human Insulin-induced weakness in hypokalemic myopathy. 496411 1979
Entrez Id: 5443
Gene Symbol: POMC
POMC
0.300 Biomarker phenotype CTD_human Mineralocorticoid hypertension in childhood. 323586 1977
Entrez Id: 5443
Gene Symbol: POMC
POMC
0.300 Biomarker phenotype CTD_human Treatment of ocular myasthenia with corticotrophin. 4323972 1971
Entrez Id: 657
Gene Symbol: BMPR1A
BMPR1A
0.100 Biomarker phenotype HPO
Entrez Id: 1586
Gene Symbol: CYP17A1
CYP17A1
0.100 Biomarker phenotype HPO
Entrez Id: 6340
Gene Symbol: SCNN1G
SCNN1G
0.100 Biomarker phenotype HPO
Entrez Id: 859
Gene Symbol: CAV3
CAV3
0.100 Biomarker phenotype HPO
Entrez Id: 6337
Gene Symbol: SCNN1A
SCNN1A
0.100 Biomarker phenotype HPO
Entrez Id: 6336
Gene Symbol: SCN10A
SCN10A
0.100 Biomarker phenotype HPO